Evidence map›Paper›PMID 37583696›Full record

ArticleFrontiers in immunology2023

Nivolumab plus Brentuximab vedotin +/- bendamustine combination therapy: a safe and effective treatment in pediatric recurrent and refractory classical Hodgkin lymphoma.

Patrick Greve, Auke Beishuizen, Melanie Hagleitner, Jan Loeffen, Margreet Veening, Marianne Boes, Victor Peperzak, Claudius Diez, Friederike Meyer-Wentrup

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.8field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Patrick GreveCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Auke BeishuizenDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Melanie HagleitnerDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Jan LoeffenDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Margreet VeeningDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Marianne BoesCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Victor PeperzakCenter for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands.
Claudius DiezDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Friederike Meyer-WentrupDepartment of Hemato-oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, Netherlands.
Princess Máxima Center · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Classical Hodgkin lymphoma (cHL) is the most common pediatric lymphoma. Approximately 10% of patients develop refractory or recurrent disease. These patients are treated with intensive chemotherapy followed by consolidation with radiotherapy or high-dose chemotherapy and autologous stem cell reinfusion. Although this treatment is effective, it comes at the cost of severe long-term adverse events, such as reduced fertility and an increased risk of secondary cancers. Recently, promising results of inducing remission with the immune checkpoint inhibitor nivolumab (targeting PD-1) and the anti-CD30 antibody-drug conjugate Brentuximab vedotin (BV) +/- bendamustine were published. Methods: Here we describe a cohort of 10 relapsed and refractory pediatric cHL patients treated with nivolumab + BV +/- bendamustine to induce remission prior to consolidation with standard treatment. Results and discussion: All patients achieved complete remission prior to consolidation treatment and are in ongoing complete remission with a median follow-up of 25 months (range: 12 to 42 months) after end-of-treatment. Only one adverse event of CTCAE grade 3 or higher due to nivolumab + BV was identified. Based on these results we conclude that immunotherapy with nivolumab + BV +/- bendamustine is an effective and safe treatment to induce remission in pediatric R/R cHL patients prior to standard consolidation treatment. We propose to evaluate this treatment further to study putative long-term toxicity and the possibility to reduce the intensity of consolidation treatment.

Indexed as

Hodgkin DiseaseBendamustine HydrochlorideBrentuximab VedotinChildHumansNivolumabTreatment OutcomeBendamustine HydrochlorideBrentuximab VedotinNivolumabcheckpoint inhibitioncombination immunotherapyoncologyrecurrent/refractory classical Hodgkin lymphomatargeted therapy

Identifiers

PMID37583696
PMCPMC10423930
OpenAlexW4385417820

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.